Package 70518-4170-0

{"route": ["ORAL"], "spl_id": "468d55bb-958e-ceae-e063-6294a90a7884", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["f6ad4729-b291-42c4-8483-99385d8043db"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0)", "package_ndc": "70518-4170-0", "marketing_start_date": "20240828"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1)", "package_ndc": "70518-4170-1", "marketing_start_date": "20250404"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2)", "package_ndc": "70518-4170-2", "marketing_start_date": "20250708"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3)", "package_ndc": "70518-4170-3", "marketing_start_date": "20251024"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-4)", "package_ndc": "70518-4170-4", "marketing_start_date": "20251222"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "70518-4170_468d55bb-958e-ceae-e063-6294a90a7884", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-4170", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20240828", "listing_expiration_date": "20261231"}